RS397515455 PLEKHG5

Health Risk Chr 1:6473051
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease recessive intermediate C
Neuronopathy
distal hereditary motor
autosomal recessive 4
Charcot-Marie-Tooth disease recessive intermediate C
Neuronopathy
distal hereditary motor
autosomal recessive 4
Other Variants in PLEKHG5
rs63750315 rs397515454 rs373184968 rs150807400 rs199794578 rs202191898 rs140202670 rs141032388 rs112530241 rs886042289
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